Transposable element‐mediated DNA methylation of the <i>NAC20</i> and <i>NAC26</i> promoters led to a maternal effect on grain filling

Parent-of-origin effects are usually caused by selective expression of maternal or paternal alleles. Although genome-wide studies suggest that imprinted gene expression occurs primarily in the endosperm in plants, detailed studies of allele-specific gene expression and its associations with parent-of-origin phenotypes are scarce. NAC20 and NAC26 (NAC20/26 hereafter), a pair of tightly linked NAC-family transcription factors, redundantly regulate grain filling and albumin accumulation in rice endosperm. Here, we show that NAC20/26 exhibited allele-specific maternal expression, and the floury endosperm phenotype of the nac20/26 double mutant was inherited with a maternal effect. Further studies showed that the imprinted NAC20/26 expression and floury endosperm phenotype with a maternal effect are associated with insertions of two TEs in NAC20/26 of two Japonica rice varieties, but not in two Indica ones examined. The maternal NAC20/26 expression was associated with elevated DNA methylation in their paternal DMRs, and deletions of those TEs by gene editing led to decreased methylation in these DMRs, and biallelic NAC20/26 expression. Geographical analyses showed that Japonica varieties with high-latitude origins examined carried these TEs. These results establish that TE-mediated DNA methylation lead to grain filling with a maternal effect in high-latitude Japonica rice varieties, which may associate with northward expansion of rice during domestication.

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Journal
Journal of Integrative Plant Biology
Published
2025-12-30
DOI
https://doi.org/10.1111/jipb.70126
Primary Topic
Plant Molecular Biology Research
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article
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article

Transposable element‐mediated DNA methylation of the NAC20 and NAC26 promoters led to a maternal effect on grain filling

Han Cheng, Jianwen Liu, Jing Zhang, Ming‐Wei Wu et al.
Journal of Integrative Plant Biology
Plant Molecular Biology Research
article

Transposable element‐mediated DNA methylation of the NAC20 and NAC26 promoters led to a maternal effect on grain filling

Han Cheng, Jianwen Liu, Jing Zhang, Ming‐Wei Wu, Wentao Wei, Ting Yang, Jin‐Lei Liu, Chunming Liu, Rong Li, Meng‐Meng Chen
article en

Abstract

Parent-of-origin effects are usually caused by selective expression of maternal or paternal alleles. Although genome-wide studies suggest that imprinted gene expression occurs primarily in the endosperm in plants, detailed studies of allele-specific gene expression and its associations with parent-of-origin phenotypes are scarce. NAC20 and NAC26 (NAC20/26 hereafter), a pair of tightly linked NAC-family transcription factors, redundantly regulate grain filling and albumin accumulation in rice endosperm. Here, we show that NAC20/26 exhibited allele-specific maternal expression, and the floury endosperm phenotype of the nac20/26 double mutant was inherited with a maternal effect. Further studies showed that the imprinted NAC20/26 expression and floury endosperm phenotype with a maternal effect are associated with insertions of two TEs in NAC20/26 of two Japonica rice varieties, but not in two Indica ones examined. The maternal NAC20/26 expression was associated with elevated DNA methylation in their paternal DMRs, and deletions of those TEs by gene editing led to decreased methylation in these DMRs, and biallelic NAC20/26 expression. Geographical analyses showed that Japonica varieties with high-latitude origins examined carried these TEs. These results establish that TE-mediated DNA methylation lead to grain filling with a maternal effect in high-latitude Japonica rice varieties, which may associate with northward expansion of rice during domestication.

Journal of Integrative Plant BiologyVol. 68(3)
Yunnan University (CN), Chinese Academy of Sciences (CN), Institute of Genetics and Developmental Biology (CN), Chinese Academy of Agricultural Sciences (CN), Institute of Botany (CN), Institute of Crop Sciences (CN), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 23%
Plant Molecular Biology Research
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